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76910-12-8

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76910-12-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76910-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,1 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76910-12:
(7*7)+(6*6)+(5*9)+(4*1)+(3*0)+(2*1)+(1*2)=138
138 % 10 = 8
So 76910-12-8 is a valid CAS Registry Number.

76910-12-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-carbonochloridoylcyclopentane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-chloroformyl-1-cyclopentane-carboxylic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76910-12-8 SDS

76910-12-8Relevant articles and documents

Use of malonic acid derivative compounds for retarding plant growth

-

, (2008/06/13)

This invention relates to a method for retarding plant growth by applying to the plant an effective amount of a malonic acid derivative compound. This invention also relates to novel malonic acid derivative compounds and processes for the preparation thereof.

Cyclit-Reaktionen, II. Darstellung von Bausteinen zur Synthese carbocyclischer Furanose-Analoga

Paulsen, Hans,Maass, Uwe

, p. 346 - 358 (2007/10/02)

The four isomeric hydroxycyclopentenmethanols 6a to 9a can easily be made by allylhydroxylation of the epoxides 2 and 4 with phenyl selenide.In a second way the pair 8a and 9a has been synthesized from 11 via 15.As the preparation of 20 demonstrates, the functionalisation of 6a to 9a to carbocyclic furanoses is possible.The dicarboxylic diethyl esters 23 and 33 can be converted into models for carbocyclic ketofuranoses.

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